Does BREXANOLONE Cause Product administration error? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product administration error have been filed in association with BREXANOLONE. This represents 13.8% of all adverse event reports for BREXANOLONE.
36
Reports of Product administration error with BREXANOLONE
13.8%
of all BREXANOLONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From BREXANOLONE?
Of the 36 reports, 1 (2.8%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXANOLONE. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does BREXANOLONE Cause?
Anxiety (34)
Drug ineffective (26)
Off label use (24)
Drug monitoring procedure incorrectly performed (19)
Fatigue (17)
Dizziness (16)
Perinatal depression (15)
Crying (14)
Product administration interrupted (14)
Feeling abnormal (13)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BREXANOLONE Alternatives Have Lower Product administration error Risk?
BREXANOLONE vs BREXPIPRAZOLE
BREXANOLONE vs BREXUCABTAGENE AUTOLEUCEL
BREXANOLONE vs BRIGATINIB
BREXANOLONE vs BRILINTA
BREXANOLONE vs BRILIQUE